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²éѯ½á¹û£º¹²²éµ½850¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-Chloro-2-(4-bromophenylcarbamoyl)phenyl acetate C15H11BrClNO3 ÏàËÆ¶È:69.2% Molecules 2007 12 1-12 Salicylanilide Acetates: Synthesis and Antibacterial Evaluation Jarmila Vinsova, Ales Imramovsky, Vladimir Buchta, Martina Ceckova, Martin Dolezal, Frantisek Staud, Josef Jampilek and Jarmila Kaustova Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1-(4-Bromophenyl)-2-(p-tolylthio)ethylacetate C17H17BrO2S ÏàËÆ¶È:69.2% Tetrahedron 2013 69 8847-8856 PhI(OAc)2/KI mediated 1,2-acetoxysulfenylation of alkenes: facile synthesis of ¦Â-acetoxysulfides Charoensak Muangkaew, Praewpan Katrun, Patcharaphon Kanchanarugee, Manat Pohmakotr, Vichai Reutrakul, Darunee Soorukram, Thaworn Jaipetch, Chutima Kuhakarn Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . acetate oil ÏàËÆ¶È:66.6% Phytochemistry 1983 22 609-610 Dehydrodieugenols from Nectandra polita Margoth Suarez, Jorge Bonilla, Aura M.P. De Diaz, Hans Achenbach Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-allylphenyl benzoate C16H14O2 ÏàËÆ¶È:66.6% Tetrahedron 2012 68 2611-2620 A general route for the stereoselective synthesis of (E)-(1-propenyl)phenyl esters by catalytic CC bond isomerization Alba E. D¨ªaz-Álvarez, Pascale Crochet, Victorio Cadierno Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-((1-(4-bromobenzyl)-1H-1,2,3-triazol-4-yl-)methyl)benzenamine C16H15BrN4 ÏàËÆ¶È:66.6% Molecules 2014 19 55-66 Pseudo-Four Component Synthesis of Mono- and Di-Benzylated-1,2,3-Triazoles Derived from Aniline Daniel Mendoza-Espinosa, Guillermo E. Negron-Silva, Leticia Lomas-Romero, Atilano Gutierrez-Carrillo and Rosa Santill¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-(4-Bromophenyl)-2-(phenylthio)ethylacetate C16H15BrO2S ÏàËÆ¶È:66.6% Tetrahedron 2013 69 8847-8856 PhI(OAc)2/KI mediated 1,2-acetoxysulfenylation of alkenes: facile synthesis of ¦Â-acetoxysulfides Charoensak Muangkaew, Praewpan Katrun, Patcharaphon Kanchanarugee, Manat Pohmakotr, Vichai Reutrakul, Darunee Soorukram, Thaworn Jaipetch, Chutima Kuhakarn Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-(4-Bromophenyl)-2-((4-fluorophenyl)thio)ethylacetate C16H14BrFO2S ÏàËÆ¶È:66.6% Tetrahedron 2013 69 8847-8856 PhI(OAc)2/KI mediated 1,2-acetoxysulfenylation of alkenes: facile synthesis of ¦Â-acetoxysulfides Charoensak Muangkaew, Praewpan Katrun, Patcharaphon Kanchanarugee, Manat Pohmakotr, Vichai Reutrakul, Darunee Soorukram, Thaworn Jaipetch, Chutima Kuhakarn Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 1,3-Diacetoxy-4,6-di(3-methyl-2-buten-1-yl) Benzene ÏàËÆ¶È:63.6% Molecules 2012 17 556-570 Synthesis and DPPH Radical Scavenging Activity of Prenylated Phenol Derivatives Mauricio Osorio, Jacqueline Aravena, Alejandra Vergara, Lautaro Taborga,Evelyn Baeza, Karen Catal¨¢n, Cesar Gonz¨¢lez, Marcela Carvajal, H¨¦ctor Carrasco and Luis Espinoza Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2c ÏàËÆ¶È:63.6% Tetrahedron Letters 2000 41 9981-9984 Cross-coupling reaction: stereoselective synthesis of (E)-aryl or heteroarylvinylgermanes Franck David-Quillot, J¨¦rôme Thibonnet, Didier Marsacq, Mohamed Abarbri, Alain Duch¨ºne Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . dehydrodieugenol acetate ÏàËÆ¶È:63.6% Phytochemistry 1988 27 3008-3009 An improved high yield synthesis of dehydrodieugenol Aderson de Farias Dias Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . macrocycle 11a C24H22O4N2 ÏàËÆ¶È:63.6% Journal of Heterocyclic Chemistry 2009 46 656-663 |
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